4.6 Article

Tipranavir resistance associated mutations in protease inhibitor-naive patients with HIV-1 subtype A/E infection

期刊

JOURNAL OF CLINICAL VIROLOGY
卷 43, 期 3, 页码 284-286

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ELSEVIER SCIENCE BV
DOI: 10.1016/j.jcv.2008.07.002

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HIV; Tipranavir; Resistance; Mutations; Subtype A/E; CRF01 AE

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资金

  1. Medicine Ramathibodi Hospital
  2. Mahidol University

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Background: Tipranavir-resistance associated mutations (TPV-RAMs) are often observed among patients with HIV-1 Subtype A/E infection. Data regarding TPV resistance in subtype A/E is still limited. Objectives: To determine the prevalence of TPV-RAMs among protease inhibitor-naive, HIV-1 subtype A/E infected patients. Study design: Genotypic resistance testing was conducted among HIV-1-infected patients who were Pl-naive. Results: We studied 112 patients (mean age, 40.7 years; 58% male). Median CD4 cell count and HIV-1 RNA were 192 cells/mm(3) and 4.2 log copies/mL, respectively. Ninety-three patients (83%) infected with subtype A/E; the others had subtype B.The most common TPV-RAMs were M361(88%), H69K (61%), and 113V(48%). Median number of TPV-RAMs was 3 mutations. Patients with subtype A/E had higher prevalence of 113V (54% vs. 21%, P=0.011), M361(96% vs. 53%, P<0.001), H69K (68% vs. 26%, P=0.001), and >2 TPV-RAMs (62% vs. 21%, P=0.002). In multivariate analysis, only subtype A/E was associated with the occurrence of >2 TPV-RAMs (OR 9.83: 95%Cl, 1.95-39.57: P=0.006). Conclusions: TPV-RAMs previously described by IAS-USA are commonly observed in Pl-naive patients with HIV-1 subtype A/E infection. Further studies to define virologic response of subtype A/E to TPV and clinical validation of TPV-RAMs in HIV-1 subtype A/E are essentially needed. (C) 2008 Elsevier B.V. All rights reserved.

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